United States · FDA National Drug Code directory

Zoledronic Acid

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
55150-283_ab56911b-70e0-46c4-a985-990244bd67bc
Product NDC
55150-283
Form
INJECTION, SOLUTION
Composition / generic term
Zoledronic Acid
Labeler
Eugia US LLC
Marketing category
ANDA
Marketing start / end (source format)
20171208
Source listing expiry
20271231

Source-listed ingredients

  • ZOLEDRONIC ACID — 5 mg/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, GLASS in 1 CARTON (55150-283-99) / 100 mL in 1 BOTTLE, GLASS · 55150-283-99

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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